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Environmental perturbation of the circadian clock during pregnancy leads to transgenerational mood disorder-like behaviors in mice

It remains unknown whether chronic circadian disturbance (CCD) during pregnancy can lead to mood disorders in the offspring. Here we show that pregnant mice in the F0 generation that were exposed to CCD stress displayed depression-like behaviors, and produced offspring in the F1 and F2 generations t...

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Autores principales: Zhang, Peng, Li, Guang, Li, Hui, Tan, XiaoQiu, Cheng, Hai-Ying Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626699/
https://www.ncbi.nlm.nih.gov/pubmed/28974783
http://dx.doi.org/10.1038/s41598-017-13067-y
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author Zhang, Peng
Li, Guang
Li, Hui
Tan, XiaoQiu
Cheng, Hai-Ying Mary
author_facet Zhang, Peng
Li, Guang
Li, Hui
Tan, XiaoQiu
Cheng, Hai-Ying Mary
author_sort Zhang, Peng
collection PubMed
description It remains unknown whether chronic circadian disturbance (CCD) during pregnancy can lead to mood disorders in the offspring. Here we show that pregnant mice in the F0 generation that were exposed to CCD stress displayed depression-like behaviors, and produced offspring in the F1 and F2 generations that also exhibited mood-associated behavioral phenotypes despite the lack of direct stressful experiences during their postnatal or adult period. Prenatal CCD stress was correlated with the elevation of plasma corticosterone levels in F1 mice. Furthermore, the diurnal expression profiles of core circadian clock genes were disrupted in the suprachiasmatic nucleus of F1 mice. Proteomics analysis revealed that prenatal CCD stress resulted in distinct changes in protein expression in the hypothalamus of female F1 mice, in particular proteins that were associated with cellular activities, metabolism, development and diseases. Sex-specific differences in melanocortin 4 receptor expression were apparent in the CCD F1 generation. We conclude that maternal exposure to chronic circadian disturbance during pregnancy can lead to sex-specific mood disorders that persist for at least two filial generations. The underlying mechanisms may depend on transgenerational changes in plasma corticosterone levels, circadian pacemaking, and hypothalamic protein expression.
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spelling pubmed-56266992017-10-12 Environmental perturbation of the circadian clock during pregnancy leads to transgenerational mood disorder-like behaviors in mice Zhang, Peng Li, Guang Li, Hui Tan, XiaoQiu Cheng, Hai-Ying Mary Sci Rep Article It remains unknown whether chronic circadian disturbance (CCD) during pregnancy can lead to mood disorders in the offspring. Here we show that pregnant mice in the F0 generation that were exposed to CCD stress displayed depression-like behaviors, and produced offspring in the F1 and F2 generations that also exhibited mood-associated behavioral phenotypes despite the lack of direct stressful experiences during their postnatal or adult period. Prenatal CCD stress was correlated with the elevation of plasma corticosterone levels in F1 mice. Furthermore, the diurnal expression profiles of core circadian clock genes were disrupted in the suprachiasmatic nucleus of F1 mice. Proteomics analysis revealed that prenatal CCD stress resulted in distinct changes in protein expression in the hypothalamus of female F1 mice, in particular proteins that were associated with cellular activities, metabolism, development and diseases. Sex-specific differences in melanocortin 4 receptor expression were apparent in the CCD F1 generation. We conclude that maternal exposure to chronic circadian disturbance during pregnancy can lead to sex-specific mood disorders that persist for at least two filial generations. The underlying mechanisms may depend on transgenerational changes in plasma corticosterone levels, circadian pacemaking, and hypothalamic protein expression. Nature Publishing Group UK 2017-10-03 /pmc/articles/PMC5626699/ /pubmed/28974783 http://dx.doi.org/10.1038/s41598-017-13067-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zhang, Peng
Li, Guang
Li, Hui
Tan, XiaoQiu
Cheng, Hai-Ying Mary
Environmental perturbation of the circadian clock during pregnancy leads to transgenerational mood disorder-like behaviors in mice
title Environmental perturbation of the circadian clock during pregnancy leads to transgenerational mood disorder-like behaviors in mice
title_full Environmental perturbation of the circadian clock during pregnancy leads to transgenerational mood disorder-like behaviors in mice
title_fullStr Environmental perturbation of the circadian clock during pregnancy leads to transgenerational mood disorder-like behaviors in mice
title_full_unstemmed Environmental perturbation of the circadian clock during pregnancy leads to transgenerational mood disorder-like behaviors in mice
title_short Environmental perturbation of the circadian clock during pregnancy leads to transgenerational mood disorder-like behaviors in mice
title_sort environmental perturbation of the circadian clock during pregnancy leads to transgenerational mood disorder-like behaviors in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626699/
https://www.ncbi.nlm.nih.gov/pubmed/28974783
http://dx.doi.org/10.1038/s41598-017-13067-y
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